Vascular plants, also called tracheophytes or collectivelyTracheophyta, form a large group of land plants that have lignified tissues for conducting water and minerals throughout the plant. They also have a specialized non-lignified tissue to conduct products of photosynthesis. Vascular plants include the clubmosses, horsetails, ferns, gymnosperms, and angiosperms. Scientific names for the group include Tracheophyta, Tracheobionta and Equisetopsida sensu lato. Some early land plants had less developed vascular tissue; the term eutracheophyte has been used for all other vascular plants, including all living ones.
Lycopodiopsida is a class of vascular plants known as lycopods, lycophytes or other terms including the component lyco-. Members of the class are also called clubmosses, firmosses, spikemosses and quillworts. They have dichotomously branching stems bearing simple leaves called microphylls and reproduce by means of spores borne in sporangia on the sides of the stems at the bases of the leaves. Although living species are small, during the Carboniferous, extinct tree-like forms (Lepidodendrales) formed huge forests that dominated the landscape and contributed to coal deposits.
Ginkgoales are a gymnosperm order containing only one extant species: Ginkgo biloba, the ginkgo tree. It is monotypic, within the class Ginkgoopsida, which itself is monotypic within the division Ginkgophytaghing-KOF-it-ə. The order includes five families, of which only Ginkgoaceae remains extant.
The lycophytes, when broadly circumscribed, are a group of vascular plants that include the clubmosses. They are sometimes placed in a division Lycopodiophyta or Lycophyta or in a subdivision Lycopodiophytina. They are one of the oldest lineages of extant (living) vascular plants; the group contains extinct plants that have been dated from the Silurian. Lycophytes were some of the dominating plant species of the Carboniferous period, and included the tree-like Lepidodendrales, some of which grew over 40 metres (130 ft) in height, although extant lycophytes are relatively small plants.
Archaeopteris is an extinct genus of progymnosperm tree with fern-like leaves. A useful index fossil, this tree is found in strata dating from the Upper Devonian to Lower Carboniferous, the oldest fossils being 385 million years old, and had global distribution.
Equisetidae is one of the four subclasses of Polypodiopsida (ferns), a group of vascular plants with a fossil record going back to the Devonian. They are commonly known as horsetails. They typically grow in wet areas, with whorls of needle-like branches radiating at regular intervals from a single vertical stem.
The progymnosperms are an extinct group of woody, spore-bearing plants that is presumed to have evolved from the trimerophytes, and eventually gave rise to the gymnosperms, ancestral to acrogymnosperms and angiosperms. They have been treated formally at the rank of division Progymnospermophyta or class Progymnospermopsida. The stratigraphically oldest known examples belong to the Middle Devonian order the Aneurophytales, with forms such as Protopteridium, in which the vegetative organs consisted of relatively loose clusters of axes. Tetraxylopteris is another example of a genus lacking leaves. In more advanced aneurophytaleans such as Aneurophyton these vegetative organs started to look rather more like fronds, and eventually during Late Devonian times the aneurophytaleans are presumed to have given rise to the pteridosperm order, the Lyginopteridales. In Late Devonian times, another group of progymnosperms gave rise to the first really large trees known as Archaeopteris. The latest surviving group of progymnosperms is the Noeggerathiales, which persisted until the end of the Permian.
The Polypodiidae, commonly called leptosporangiate ferns, formerly Leptosporangiatae, are one of four subclasses of ferns, the largest of these being the largest group of living ferns, including some 11,000 species worldwide. The group has also been treated as the class Pteridopsida or Polypodiopsida, although other classifications assign them a different rank. Older names for the group include Filicidae and Filicales, although at least the "water ferns" were then treated separately.
The cladoxylopsids are an extinct group of plants related to ferns and sphenopsids.
Psilophyton is a genus of extinct vascular plants. Described in 1859, it was one of the first fossil plants to be found which was of Devonian age. Specimens have been found in northern Maine, USA; Gaspé Bay, Quebec and New Brunswick, Canada; the Czech Republic; and Yunnan, China. Plants lacked leaves or true roots; spore-forming organs or sporangia were borne on the ends of branched clusters. It is significantly more complex than some other plants of comparable age and is thought to be part of the group from within which the modern ferns and seed plants evolved.
Polysporangiophytes, also called polysporangiates or formally Polysporangiophyta, are plants in which the spore-bearing generation (sporophyte) has branching stems (axes) that bear sporangia. The name literally means 'many sporangia plant'. The clade includes all land plants (embryophytes) except for the bryophytes whose sporophytes are normally unbranched, even if a few exceptional cases occur. While the definition is independent of the presence of vascular tissue, all living polysporangiophytes also have vascular tissue, i.e., are vascular plants or tracheophytes. Extinct polysporangiophytes are known that have no vascular tissue and so are not tracheophytes.
Lepidodendrales or arborescent lycophytes are an extinct order of primitive, vascular, heterosporous, arborescent (tree-like) plants belonging to Lycopodiopsida. Members of Lepidodendrales are the best understood of the fossil lycopsids due to the vast diversity of Lepidodendrales specimens and the diversity in which they were preserved; the extensive distribution of Lepidodendrales specimens as well as their well-preservedness lends paleobotanists exceptionally detailed knowledge of the coal-swamp giants’ reproductive biology, vegetative development, and role in their paleoecosystem. The defining characteristics of the Lepidodendrales are their secondary xylem, extensive periderm development, three-zoned cortex, rootlike appendages known as stigmarian rootlets arranged in a spiralling pattern, and megasporangium each containing a single functional megaspore that germinates inside the sporangium. Many of these different plant organs have been assigned both generic and specific names as relatively few have been found organically attached to each other. Some specimens have been discovered which indicate heights of 40 and even 50 meters and diameters of over 2 meters at the base. The massive trunks of some species branched profusely, producing large crowns of leafy twigs; though some leaves were up to 1 meter long, most were much shorter, and when leaves dropped from branches their conspicuous leaf bases remained on the surface of branches. Strobili could be found at the tips of distal branches or in an area at the top of the main trunk. The underground organs of Lepidodendrales typically consisted of dichotomizing axes bearing helically arranged, lateral appendages serving an equivalent function to roots. Sometimes called "giant club mosses", they are believed to be more closely related to extant quillworts based on xylem, although fossil specimens of extinct Selaginellales from the Late Carboniferous also had secondary xylem.
Pertica is a genus of extinct vascular plants of the Early to Middle Devonian. It has been placed in the "trimerophytes", a strongly paraphyletic group of early members of the lineage leading to modern ferns and seed plants.
Sphenophyllales is an extinct order of articulate land plants and a sister group to the present-day Equisetales (horsetails). They are fossils dating from the Devonian to the Triassic. They were common during the Late Pennsylvanian to Early Permian, with most of the fossils coming from the Carboniferous period.
Psilophytopsida is a now obsolete class containing one order, Psilophytales, which was previously used to classify a number of extinct plants which are now placed elsewhere. The class was established in 1917, under the name Psilophyta, with only three genera for a group of fossil plants from the Upper Silurian and Devonian periods which lack true roots and leaves, but have a vascular system within a branching cylindrical stem. The living Psilotaceae, the whisk-ferns, were sometimes added to the class, which was then usually called Psilopsida. This classification is no longer in use.
Tetraxylopteris is a genus of extinct vascular plants of the Middle to Upper Devonian. Fossils were first found in New York State, USA. A second species was later found in Venezuela.
Taeniocrada is a genus of extinct plants of Devonian age. It is used as a form genus for fossil plants with leafless flattened stems which divided dichotomously and had prominent midribs regarded as containing vascular tissues. It has been suggested that some species assigned to this genus were aquatic.
Rotafolia songziensis is a species of the extinct Sphenophyllales horsetails.
Calamopityaceae is the largest family of the division of extinct seed-bearing plants (spermatophytes) known as Pteridospermatophyta. It is the only family in the monotypic order Calamopityales. This family is characterized by its petioles and specific wood pattern, and it grew only in the Paleozoic era, specifically in North America and Europe. Three form genera within the family are diagnosed by their stem structure: Calamopitys, Stenomyelon, and Diichinia. It was named by Solms-Laubach in 1896. Since then, its genera have been added to and grouped differently.
The barinophytes are a group of extinct vascular plants (tracheophytes). Their relationship with other vascular plants is unclear. They have been treated as the separate class Barinophytopsida, the order Barinophytales of uncertain class and as a family or clade Barinophytaceae within the zosterophylls. They have also been considered to be possible lycopodiopsids.
Thomas N. Taylor, Edith L. Taylor, Michael Krings: Paleobotany. The Biology and Evolution of Fossil Plants . Second Edition, Academic Press 2009, ISBN 978-0-12-373972-8, p. 401-405.
